chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	24446969	24446970	A	G	24	GENIC	homozygous	46392843
18	24447142	24447143	A	G	36	GENIC	homozygous	46392845
18	24447609	24447610	G	A	36	GENIC	homozygous	46392847
18	24448319	24448320	C	T	42	GENIC	homozygous	46931064
18	24449165	24449166	G	T	28	GENIC	homozygous	46931065
18	24449526	24449527	G	A	29	GENIC	homozygous	46392849
18	24450193	24450194	A	G	22	GENIC	homozygous	46392850
18	24450490	24450491	C	T	30	GENIC	homozygous	46392851
18	24451010	24451011	T	C	31	GENIC	homozygous	46392852
18	24451633	24451634	G	T	30	GENIC	homozygous	46931066
18	24452586	24452587	G	A	52	GENIC	homozygous	46931067
18	24452605	24452606	G	GGT	11	GENIC	possibly homozygous	46896632
18	24453055	24453056	G	T	30	GENIC	homozygous	46931068
18	24453161	24453162	T	TA	37	GENIC	homozygous	46931069
18	24453165	24453166	T	A	41	GENIC	homozygous	46931070
18	24453314	24453315	C	CTTT	11	GENIC	heterozygous	46392854
18	24453314	24453315	C	CTTTT	11	GENIC	possibly homozygous	46896633